Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g34030 A02 29152851 C T upstream_gene_variant MODIFIER c.-4613C>T| S295
2 BAA02g34030 A02 29154808 C T upstream_gene_variant MODIFIER c.-2656C>T| S261
3 BAA02g34030 A02 29155654 G A upstream_gene_variant MODIFIER c.-1810G>A| S209
4 BAA02g34030 A02 29155810 G A upstream_gene_variant MODIFIER c.-1654G>A| S35
5 BAA02g34030 A02 29158171 G A intron_variant MODIFIER c.449+259G>A| S71
6 BAA02g34030 A02 29158526 C T intron_variant MODIFIER c.449+614C>T| S55
7 BAA02g34030 A02 29158611 C T intron_variant MODIFIER c.449+699C>T| S135
8 BAA02g34030 A02 29159594 G A intron_variant MODIFIER c.449+1682G>A| S5
9 BAA02g34030 A02 29159600 G A intron_variant MODIFIER c.449+1688G>A| S196
10 BAA02g34030 A02 29159973 C T intron_variant MODIFIER c.449+2061C>T| S295
11 BAA02g34030 A02 29160318 G A intron_variant MODIFIER c.450-2176G>A| S132
S137
S215
S89
12 BAA02g34030 A02 29160430 C T intron_variant MODIFIER c.450-2064C>T| S138
13 BAA02g34030 A02 29161133 G A intron_variant MODIFIER c.450-1361G>A| S96
14 BAA02g34030 A02 29161302 G A intron_variant MODIFIER c.450-1192G>A| S86
15 BAA02g34030 A02 29162057 C T intron_variant MODIFIER c.450-437C>T| S202
16 BAA02g34030 A02 29162513 G A missense_variant MODERATE c.469G>A|p.Glu157Lys S70
17 BAA02g34030 A02 29163605 C T synonymous_variant LOW c.1561C>T|p.Leu521Leu S178
18 BAA02g34030 A02 29163780 C T intron_variant MODIFIER c.1629+107C>T| S167
19 BAA02g34030 A02 29164240 G A stop_gained HIGH c.1809G>A|p.Trp603* S225
S73